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Cited by in F6Publishing
For: Marini SC, Gomes M, Guilherme R, Carda JP, Pinto CS, Fidalgo T, Ribeiro ML. Atypical hemolytic-uremic syndrome: recurrent phenotypic expression of a patient with MCP gene mutation combined with risk haplotypes. Blood Coagul Fibrinolysis 2019;30:68-70. [PMID: 30676336 DOI: 10.1097/MBC.0000000000000793] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
Number Citing Articles
1 Ren Z, Perkins SJ, Love-Gregory L, Atkinson JP, Java A. Clinicopathologic Implications of Complement Genetic Variants in Kidney Transplantation. Front Med (Lausanne) 2021;8:775280. [PMID: 34912830 DOI: 10.3389/fmed.2021.775280] [Reference Citation Analysis]
2 van den Broek B, van der Flier M, de Groot R, de Jonge MI, Langereis JD. Common Genetic Variants in the Complement System and their Potential Link with Disease Susceptibility and Outcome of Invasive Bacterial Infection. J Innate Immun 2020;12:131-41. [PMID: 31269507 DOI: 10.1159/000500545] [Cited by in Crossref: 1] [Cited by in F6Publishing: 3] [Article Influence: 0.3] [Reference Citation Analysis]